Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
T |
11: 9,285,232 (GRCm39) |
T3289S |
probably damaging |
Het |
Actr1b |
G |
T |
1: 36,740,534 (GRCm39) |
Q240K |
probably benign |
Het |
Adamts19 |
T |
C |
18: 59,034,048 (GRCm39) |
V341A |
probably damaging |
Het |
Akirin2 |
C |
A |
4: 34,551,148 (GRCm39) |
S35* |
probably null |
Het |
Alg3 |
G |
T |
16: 20,427,765 (GRCm39) |
Q90K |
probably benign |
Het |
Alox12 |
C |
T |
11: 70,138,153 (GRCm39) |
R394H |
possibly damaging |
Het |
Ankrd17 |
A |
C |
5: 90,411,134 (GRCm39) |
M1387R |
probably damaging |
Het |
Anp32b |
T |
G |
4: 46,468,592 (GRCm39) |
F121V |
possibly damaging |
Het |
Atp2b2 |
A |
G |
6: 113,740,566 (GRCm39) |
V815A |
probably damaging |
Het |
Atxn7l1 |
T |
C |
12: 33,417,420 (GRCm39) |
L527S |
probably benign |
Het |
B9d2 |
C |
T |
7: 25,385,462 (GRCm39) |
L91F |
possibly damaging |
Het |
Bcl2l11 |
T |
A |
2: 128,000,221 (GRCm39) |
I188N |
probably damaging |
Het |
Bnc2 |
A |
C |
4: 84,210,138 (GRCm39) |
S744A |
probably benign |
Het |
Casr |
T |
G |
16: 36,330,414 (GRCm39) |
M307L |
probably benign |
Het |
Cd109 |
CATTTATTTATTTATTTATTTATTTATTTATTTAT |
CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT |
9: 78,619,782 (GRCm39) |
|
probably benign |
Het |
Cd109 |
TTATA |
TTATATATA |
9: 78,619,813 (GRCm39) |
|
probably benign |
Het |
Cd22 |
A |
G |
7: 30,575,449 (GRCm39) |
S198P |
probably benign |
Het |
Cd37 |
C |
A |
7: 44,886,622 (GRCm39) |
V99L |
probably benign |
Het |
Cdkn1c |
A |
G |
7: 143,013,964 (GRCm39) |
S161P |
possibly damaging |
Het |
Chi3l1 |
G |
T |
1: 134,111,919 (GRCm39) |
|
probably null |
Het |
Col4a2 |
T |
C |
8: 11,498,198 (GRCm39) |
F1669S |
probably damaging |
Het |
Dchs2 |
A |
T |
3: 83,261,493 (GRCm39) |
H2587L |
probably benign |
Het |
Ddx19a |
A |
T |
8: 111,710,228 (GRCm39) |
M124K |
probably benign |
Het |
Dnhd1 |
A |
T |
7: 105,341,933 (GRCm39) |
H1244L |
possibly damaging |
Het |
Dnpep |
G |
A |
1: 75,292,329 (GRCm39) |
P165L |
probably damaging |
Het |
Dpp3 |
T |
C |
19: 4,973,172 (GRCm39) |
R141G |
probably benign |
Het |
Dpysl3 |
T |
C |
18: 43,462,814 (GRCm39) |
D521G |
probably damaging |
Het |
Dusp4 |
T |
A |
8: 35,284,345 (GRCm39) |
M220K |
probably damaging |
Het |
Duxf4 |
G |
A |
10: 58,071,711 (GRCm39) |
P168S |
probably damaging |
Het |
Edc4 |
T |
A |
8: 106,613,833 (GRCm39) |
L391Q |
probably damaging |
Het |
Edrf1 |
A |
C |
7: 133,273,207 (GRCm39) |
I1221L |
probably benign |
Het |
Elavl2 |
A |
G |
4: 91,199,847 (GRCm39) |
L12P |
probably benign |
Het |
Fastkd3 |
T |
A |
13: 68,733,071 (GRCm39) |
V464D |
probably damaging |
Het |
Flt4 |
C |
A |
11: 49,527,598 (GRCm39) |
N920K |
probably benign |
Het |
Gimap3 |
T |
C |
6: 48,742,259 (GRCm39) |
T224A |
probably benign |
Het |
Gm9772 |
T |
A |
17: 22,225,565 (GRCm39) |
K112* |
probably null |
Het |
Gp5 |
C |
A |
16: 30,127,976 (GRCm39) |
V233L |
|
Het |
Gpr25 |
A |
T |
1: 136,188,026 (GRCm39) |
W196R |
probably benign |
Het |
Hs3st4 |
G |
A |
7: 123,582,680 (GRCm39) |
G93S |
probably damaging |
Het |
Igsf10 |
A |
G |
3: 59,236,668 (GRCm39) |
L1171S |
probably benign |
Het |
Itgb7 |
C |
T |
15: 102,126,359 (GRCm39) |
G526S |
possibly damaging |
Het |
Kcnh8 |
G |
A |
17: 53,141,642 (GRCm39) |
C295Y |
probably damaging |
Het |
Klhl8 |
A |
G |
5: 104,015,709 (GRCm39) |
|
probably null |
Het |
Krt1c |
T |
A |
15: 101,726,317 (GRCm39) |
I74F |
unknown |
Het |
Lamp5 |
G |
T |
2: 135,911,054 (GRCm39) |
M262I |
probably benign |
Het |
Lrp5 |
G |
T |
19: 3,680,156 (GRCm39) |
R443S |
possibly damaging |
Het |
Lrrc66 |
G |
T |
5: 73,765,267 (GRCm39) |
A592E |
probably benign |
Het |
Lrrc66 |
C |
T |
5: 73,765,268 (GRCm39) |
A592T |
probably benign |
Het |
Mettl23 |
T |
A |
11: 116,744,865 (GRCm39) |
V93D |
unknown |
Het |
Mier2 |
G |
A |
10: 79,384,274 (GRCm39) |
R166W |
probably damaging |
Het |
Mkrn2os |
G |
A |
6: 115,562,325 (GRCm39) |
R213W |
probably benign |
Het |
Mrps36 |
T |
A |
13: 100,877,715 (GRCm39) |
I22L |
probably damaging |
Het |
Msantd5f4 |
A |
G |
4: 73,557,185 (GRCm39) |
N6S |
possibly damaging |
Het |
Myocd |
T |
C |
11: 65,077,795 (GRCm39) |
R667G |
probably benign |
Het |
Ncapg |
T |
A |
5: 45,853,140 (GRCm39) |
L869M |
probably damaging |
Het |
Ndst3 |
T |
C |
3: 123,465,549 (GRCm39) |
N141S |
probably benign |
Het |
Neu2 |
A |
T |
1: 87,524,965 (GRCm39) |
R317* |
probably null |
Het |
Nf1 |
G |
T |
11: 79,364,168 (GRCm39) |
V1533F |
probably damaging |
Het |
Npy4r |
T |
A |
14: 33,869,083 (GRCm39) |
R68S |
possibly damaging |
Het |
Nr1h5 |
T |
C |
3: 102,853,427 (GRCm39) |
H360R |
probably null |
Het |
Or1x6 |
G |
A |
11: 50,938,938 (GRCm39) |
M1I |
probably null |
Het |
Or4f14c |
T |
C |
2: 111,941,441 (GRCm39) |
D52G |
probably damaging |
Het |
Or9s15 |
T |
C |
1: 92,524,978 (GRCm39) |
S246P |
probably damaging |
Het |
Osmr |
A |
C |
15: 6,882,027 (GRCm39) |
V39G |
probably damaging |
Het |
Plekhm2 |
T |
C |
4: 141,359,732 (GRCm39) |
D345G |
possibly damaging |
Het |
Prkaa2 |
G |
T |
4: 104,906,600 (GRCm39) |
S165* |
probably null |
Het |
Qser1 |
A |
T |
2: 104,593,292 (GRCm39) |
F1575Y |
possibly damaging |
Het |
Rasl11a |
C |
A |
5: 146,782,107 (GRCm39) |
D27E |
probably benign |
Het |
Ret |
A |
T |
6: 118,142,888 (GRCm39) |
Y929* |
probably null |
Het |
Samd9l |
T |
A |
6: 3,373,493 (GRCm39) |
E1256V |
probably benign |
Het |
Scnn1g |
A |
G |
7: 121,341,566 (GRCm39) |
I243V |
possibly damaging |
Het |
Slc6a3 |
C |
T |
13: 73,718,031 (GRCm39) |
R514* |
probably null |
Het |
Sorcs3 |
C |
T |
19: 48,194,809 (GRCm39) |
A64V |
probably benign |
Het |
Sos1 |
G |
T |
17: 80,715,723 (GRCm39) |
N1011K |
probably benign |
Het |
Srbd1 |
C |
A |
17: 86,428,115 (GRCm39) |
A373S |
possibly damaging |
Het |
Tas1r1 |
C |
T |
4: 152,122,833 (GRCm39) |
W4* |
probably null |
Het |
Tcf15 |
C |
T |
2: 151,985,690 (GRCm39) |
R49C |
probably damaging |
Het |
Tex30 |
A |
G |
1: 44,127,136 (GRCm39) |
V124A |
possibly damaging |
Het |
Tgif1 |
T |
C |
17: 71,151,882 (GRCm39) |
D243G |
|
Het |
Tgtp1 |
T |
G |
11: 48,877,916 (GRCm39) |
D263A |
probably damaging |
Het |
Themis3 |
T |
A |
17: 66,862,864 (GRCm39) |
T365S |
probably benign |
Het |
Thoc2l |
C |
A |
5: 104,666,818 (GRCm39) |
P447T |
probably benign |
Het |
Tprg1 |
A |
T |
16: 25,231,662 (GRCm39) |
I213F |
probably damaging |
Het |
Traf4 |
A |
T |
11: 78,052,005 (GRCm39) |
C160S |
probably damaging |
Het |
Trio |
T |
C |
15: 27,732,770 (GRCm39) |
E3037G |
possibly damaging |
Het |
Ttbk2 |
G |
T |
2: 120,575,911 (GRCm39) |
S1022* |
probably null |
Het |
Ttn |
A |
C |
2: 76,549,452 (GRCm39) |
Y31742D |
probably benign |
Het |
Ttn |
G |
T |
2: 76,617,595 (GRCm39) |
P16292Q |
probably damaging |
Het |
Ubr5 |
A |
G |
15: 38,002,503 (GRCm39) |
V1510A |
|
Het |
Vac14 |
A |
G |
8: 111,379,869 (GRCm39) |
D389G |
probably benign |
Het |
Vwa8 |
A |
G |
14: 79,324,150 (GRCm39) |
D1151G |
probably benign |
Het |
Zfp608 |
T |
C |
18: 55,032,266 (GRCm39) |
N558S |
probably damaging |
Het |
|
Other mutations in Ttc6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03278:Ttc6
|
APN |
12 |
57,668,812 (GRCm39) |
missense |
probably damaging |
0.99 |
polonius
|
UTSW |
12 |
57,704,928 (GRCm39) |
splice site |
probably null |
|
tybalt
|
UTSW |
12 |
57,720,542 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02802:Ttc6
|
UTSW |
12 |
57,622,654 (GRCm39) |
missense |
probably benign |
0.14 |
PIT4802001:Ttc6
|
UTSW |
12 |
57,772,462 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0698:Ttc6
|
UTSW |
12 |
57,720,002 (GRCm39) |
missense |
probably benign |
0.04 |
R0988:Ttc6
|
UTSW |
12 |
57,735,435 (GRCm39) |
splice site |
probably benign |
|
R1290:Ttc6
|
UTSW |
12 |
57,707,199 (GRCm39) |
missense |
probably benign |
0.00 |
R1338:Ttc6
|
UTSW |
12 |
57,663,155 (GRCm39) |
missense |
probably benign |
0.10 |
R1468:Ttc6
|
UTSW |
12 |
57,721,463 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1468:Ttc6
|
UTSW |
12 |
57,721,463 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1481:Ttc6
|
UTSW |
12 |
57,783,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R1488:Ttc6
|
UTSW |
12 |
57,696,301 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1558:Ttc6
|
UTSW |
12 |
57,733,132 (GRCm39) |
missense |
probably benign |
0.14 |
R1570:Ttc6
|
UTSW |
12 |
57,721,549 (GRCm39) |
missense |
probably damaging |
0.98 |
R1619:Ttc6
|
UTSW |
12 |
57,784,454 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1819:Ttc6
|
UTSW |
12 |
57,741,286 (GRCm39) |
critical splice donor site |
probably null |
|
R1826:Ttc6
|
UTSW |
12 |
57,707,033 (GRCm39) |
missense |
probably benign |
0.10 |
R1863:Ttc6
|
UTSW |
12 |
57,760,881 (GRCm39) |
missense |
probably benign |
0.04 |
R1872:Ttc6
|
UTSW |
12 |
57,751,338 (GRCm39) |
critical splice donor site |
probably null |
|
R1887:Ttc6
|
UTSW |
12 |
57,720,044 (GRCm39) |
missense |
probably benign |
0.04 |
R1937:Ttc6
|
UTSW |
12 |
57,663,109 (GRCm39) |
missense |
probably benign |
0.02 |
R2014:Ttc6
|
UTSW |
12 |
57,623,003 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2056:Ttc6
|
UTSW |
12 |
57,784,479 (GRCm39) |
missense |
probably benign |
0.08 |
R2058:Ttc6
|
UTSW |
12 |
57,784,479 (GRCm39) |
missense |
probably benign |
0.08 |
R2059:Ttc6
|
UTSW |
12 |
57,784,479 (GRCm39) |
missense |
probably benign |
0.08 |
R2152:Ttc6
|
UTSW |
12 |
57,752,338 (GRCm39) |
missense |
probably damaging |
0.98 |
R2179:Ttc6
|
UTSW |
12 |
57,719,904 (GRCm39) |
missense |
possibly damaging |
0.62 |
R2275:Ttc6
|
UTSW |
12 |
57,749,084 (GRCm39) |
missense |
probably benign |
0.01 |
R2432:Ttc6
|
UTSW |
12 |
57,668,821 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2474:Ttc6
|
UTSW |
12 |
57,622,713 (GRCm39) |
missense |
probably benign |
0.37 |
R2853:Ttc6
|
UTSW |
12 |
57,622,967 (GRCm39) |
missense |
probably damaging |
0.96 |
R3848:Ttc6
|
UTSW |
12 |
57,723,932 (GRCm39) |
missense |
probably damaging |
0.97 |
R3853:Ttc6
|
UTSW |
12 |
57,775,335 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3950:Ttc6
|
UTSW |
12 |
57,696,292 (GRCm39) |
missense |
probably damaging |
0.97 |
R3953:Ttc6
|
UTSW |
12 |
57,744,238 (GRCm39) |
missense |
probably benign |
0.03 |
R3954:Ttc6
|
UTSW |
12 |
57,744,238 (GRCm39) |
missense |
probably benign |
0.03 |
R3955:Ttc6
|
UTSW |
12 |
57,744,238 (GRCm39) |
missense |
probably benign |
0.03 |
R3957:Ttc6
|
UTSW |
12 |
57,744,238 (GRCm39) |
missense |
probably benign |
0.03 |
R4135:Ttc6
|
UTSW |
12 |
57,679,581 (GRCm39) |
intron |
probably benign |
|
R4387:Ttc6
|
UTSW |
12 |
57,689,836 (GRCm39) |
missense |
probably benign |
0.00 |
R4577:Ttc6
|
UTSW |
12 |
57,623,441 (GRCm39) |
missense |
probably benign |
0.22 |
R4747:Ttc6
|
UTSW |
12 |
57,721,478 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4779:Ttc6
|
UTSW |
12 |
57,776,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R4803:Ttc6
|
UTSW |
12 |
57,775,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R4871:Ttc6
|
UTSW |
12 |
57,749,142 (GRCm39) |
missense |
probably damaging |
0.96 |
R4898:Ttc6
|
UTSW |
12 |
57,707,026 (GRCm39) |
missense |
probably benign |
0.00 |
R4930:Ttc6
|
UTSW |
12 |
57,720,609 (GRCm39) |
critical splice donor site |
probably null |
|
R4946:Ttc6
|
UTSW |
12 |
57,689,926 (GRCm39) |
missense |
probably benign |
0.01 |
R5257:Ttc6
|
UTSW |
12 |
57,749,061 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5303:Ttc6
|
UTSW |
12 |
57,622,606 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5385:Ttc6
|
UTSW |
12 |
57,689,821 (GRCm39) |
splice site |
probably null |
|
R5402:Ttc6
|
UTSW |
12 |
57,783,817 (GRCm39) |
nonsense |
probably null |
|
R5428:Ttc6
|
UTSW |
12 |
57,736,620 (GRCm39) |
missense |
probably null |
0.98 |
R5436:Ttc6
|
UTSW |
12 |
57,721,380 (GRCm39) |
splice site |
probably null |
|
R5646:Ttc6
|
UTSW |
12 |
57,622,805 (GRCm39) |
missense |
probably damaging |
0.99 |
R5697:Ttc6
|
UTSW |
12 |
57,724,000 (GRCm39) |
missense |
probably benign |
0.22 |
R5792:Ttc6
|
UTSW |
12 |
57,719,990 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5808:Ttc6
|
UTSW |
12 |
57,664,397 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5842:Ttc6
|
UTSW |
12 |
57,783,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R5935:Ttc6
|
UTSW |
12 |
57,720,590 (GRCm39) |
missense |
probably damaging |
0.98 |
R6144:Ttc6
|
UTSW |
12 |
57,719,886 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6155:Ttc6
|
UTSW |
12 |
57,784,402 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6283:Ttc6
|
UTSW |
12 |
57,749,048 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6371:Ttc6
|
UTSW |
12 |
57,775,249 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6715:Ttc6
|
UTSW |
12 |
57,721,556 (GRCm39) |
critical splice donor site |
probably null |
|
R6738:Ttc6
|
UTSW |
12 |
57,735,426 (GRCm39) |
missense |
probably damaging |
0.99 |
R6795:Ttc6
|
UTSW |
12 |
57,751,199 (GRCm39) |
missense |
probably damaging |
0.96 |
R6959:Ttc6
|
UTSW |
12 |
57,704,928 (GRCm39) |
splice site |
probably null |
|
R7053:Ttc6
|
UTSW |
12 |
57,707,318 (GRCm39) |
missense |
probably benign |
0.01 |
R7125:Ttc6
|
UTSW |
12 |
57,623,125 (GRCm39) |
missense |
probably benign |
0.00 |
R7259:Ttc6
|
UTSW |
12 |
57,622,970 (GRCm39) |
missense |
probably benign |
0.00 |
R7304:Ttc6
|
UTSW |
12 |
57,622,837 (GRCm39) |
missense |
probably damaging |
0.96 |
R7369:Ttc6
|
UTSW |
12 |
57,719,717 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7409:Ttc6
|
UTSW |
12 |
57,743,772 (GRCm39) |
missense |
probably damaging |
0.99 |
R7429:Ttc6
|
UTSW |
12 |
57,704,888 (GRCm39) |
missense |
probably benign |
0.00 |
R7430:Ttc6
|
UTSW |
12 |
57,704,888 (GRCm39) |
missense |
probably benign |
0.00 |
R7492:Ttc6
|
UTSW |
12 |
57,719,922 (GRCm39) |
missense |
probably benign |
0.02 |
R7535:Ttc6
|
UTSW |
12 |
57,623,305 (GRCm39) |
missense |
probably benign |
0.00 |
R7866:Ttc6
|
UTSW |
12 |
57,721,435 (GRCm39) |
missense |
probably damaging |
0.97 |
R7901:Ttc6
|
UTSW |
12 |
57,735,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R7944:Ttc6
|
UTSW |
12 |
57,707,229 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7945:Ttc6
|
UTSW |
12 |
57,707,229 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7965:Ttc6
|
UTSW |
12 |
57,720,542 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8062:Ttc6
|
UTSW |
12 |
57,783,764 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8119:Ttc6
|
UTSW |
12 |
57,752,429 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8142:Ttc6
|
UTSW |
12 |
57,744,258 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8154:Ttc6
|
UTSW |
12 |
57,776,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R8171:Ttc6
|
UTSW |
12 |
57,720,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R8335:Ttc6
|
UTSW |
12 |
57,707,077 (GRCm39) |
missense |
probably benign |
0.00 |
R8343:Ttc6
|
UTSW |
12 |
57,707,282 (GRCm39) |
missense |
possibly damaging |
0.47 |
R8696:Ttc6
|
UTSW |
12 |
57,784,492 (GRCm39) |
missense |
probably benign |
0.20 |
R8875:Ttc6
|
UTSW |
12 |
57,776,194 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8875:Ttc6
|
UTSW |
12 |
57,751,199 (GRCm39) |
missense |
probably damaging |
0.96 |
R8876:Ttc6
|
UTSW |
12 |
57,784,489 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8924:Ttc6
|
UTSW |
12 |
57,697,790 (GRCm39) |
nonsense |
probably null |
|
R8944:Ttc6
|
UTSW |
12 |
57,689,826 (GRCm39) |
missense |
|
|
R8956:Ttc6
|
UTSW |
12 |
57,775,196 (GRCm39) |
nonsense |
probably null |
|
R9009:Ttc6
|
UTSW |
12 |
57,744,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R9020:Ttc6
|
UTSW |
12 |
57,752,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R9232:Ttc6
|
UTSW |
12 |
57,776,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R9291:Ttc6
|
UTSW |
12 |
57,622,730 (GRCm39) |
missense |
probably damaging |
0.99 |
R9304:Ttc6
|
UTSW |
12 |
57,776,117 (GRCm39) |
missense |
probably damaging |
0.99 |
R9309:Ttc6
|
UTSW |
12 |
57,753,649 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9331:Ttc6
|
UTSW |
12 |
57,720,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R9398:Ttc6
|
UTSW |
12 |
57,784,404 (GRCm39) |
nonsense |
probably null |
|
R9430:Ttc6
|
UTSW |
12 |
57,733,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R9632:Ttc6
|
UTSW |
12 |
57,664,299 (GRCm39) |
missense |
probably benign |
|
R9688:Ttc6
|
UTSW |
12 |
57,720,602 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9732:Ttc6
|
UTSW |
12 |
57,775,335 (GRCm39) |
missense |
probably benign |
0.36 |
R9740:Ttc6
|
UTSW |
12 |
57,736,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R9749:Ttc6
|
UTSW |
12 |
57,701,559 (GRCm39) |
missense |
probably benign |
0.00 |
X0021:Ttc6
|
UTSW |
12 |
57,622,904 (GRCm39) |
missense |
probably damaging |
0.96 |
X0058:Ttc6
|
UTSW |
12 |
57,753,637 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Ttc6
|
UTSW |
12 |
57,744,161 (GRCm39) |
missense |
probably benign |
0.08 |
|